Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1003900980
Device Listing 1003900980
Listing Summary
#
Listing key
1003900980
Premarket submission
K122640
Device
VPULSE
Applicant
Cothera, LLC
Product code
JOW
Decision date
2013-02-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
155283
3010246951
3010246951
Monique Zamora
1
N
2026-01-01
2382 Faraday Avenue Suite 300 Carlsbad CA US 92008